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Complete 1H (600 MHz) and 13C NMR spectral assignments of 3,4-bis [(3,4-dimethoxyphenyl)-methyl]dihydro-(3R-trans)-2(3H)-furanone (matairesinol dimethyl ether), a naturally occurring dibenzylbutyrolactone lignan

✍ Scribed by Stefano Chimichi; Barbara Cosimelli; Massimo Bambagiotti-Alberti; Silvia A. Coran; Franco F. Vincieri


Book ID
102526854
Publisher
John Wiley and Sons
Year
1993
Tongue
English
Weight
358 KB
Volume
31
Category
Article
ISSN
0749-1581

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✦ Synopsis


Abstract

The concerted applications of a variety of one‐ and two‐dimensional NMR techniques (COSY, NOESY, HETCOR, COLOC, etc.) to the structural elucidation of the natural 3,4‐bis[(3,4‐dimethoxyphenyl)methyl]dihydro‐(3__R__‐trans)‐2(3__H__)‐furanone, isolated from Oenanthe aquatica fruits, in CDCl~3~ solution are reported. The magnitude of the ^1^H,^1^H coupling constants obtained from the simulated spectrum together with a series of homonuclear NOE difference spectra were used to determine the full stereochemistry of the system.